A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046803



Internal ID20613843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46453401..46459700hg38UCSC Ensembl
chr19:46956658..46962957hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520468
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00515


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